NBBCC   Click here for help

GtoPdb Ligand ID: 2374

Synonyms: n-butyl-β-carboline-3-carboxylate | n-butyl-beta-carboline-3-carboxylate
Compound class: Synthetic organic
Comment: This compound is represented on ChEMBL by the entry CHEMBL148296 which shows the double bonds in different positions.
2D Structure
Click here for help
Click here for structure editor
Physico-chemical Properties
Click here for help
Hydrogen bond acceptors 3
Hydrogen bond donors 1
Rotatable bonds 5
Topological polar surface area 54.98
Molecular weight 268.12
XLogP 3.65
No. Lipinski's rules broken 0

Generated using the Chemistry Development Kit (CDK) (Willighagen EL et al. Journal of Cheminformatics vol. 9:33. 2017, doi:10.1186/s13321-017-0220-4; https://cdk.github.io/)

SMILES / InChI / InChIKey
Click here for help
Canonical SMILES CCCCOC(=O)c1ncc2c(c1)c1ccccc1[nH]2
Isomeric SMILES CCCCOC(=O)c1ncc2c(c1)c1ccccc1[nH]2
InChI InChI=1S/C16H16N2O2/c1-2-3-8-20-16(19)14-9-12-11-6-4-5-7-13(11)18-15(12)10-17-14/h4-7,9-10,18H,2-3,8H2,1H3
InChI Key WGNGIELOOKACSB-UHFFFAOYSA-N

Generated using the Chemistry Development Kit (CDK) (Willighagen EL et al. Journal of Cheminformatics vol. 9:33. 2017, doi:10.1186/s13321-017-0220-4; https://cdk.github.io/)

References
1. Mangin JM, Nguyen L, Gougnard C, Hans G, Rogister B, Belachew S, Moonen G, Legendre P, Rigo JM. (2005)
Developmental regulation of beta-carboline-induced inhibition of glycine-evoked responses depends on glycine receptor beta subunit expression.
Mol Pharmacol, 67 (5): 1783-96. [PMID:15722459]